Deletions in the 3′ part of the NFIX gene including a recurrent alu-mediated deletion of exon 6 and 7 account for previously unexplained cases of marshall-smith syndrome

Denny Schanze, Dorothée Neubauer, Valerie Cormier-Daire, Marie Ange Delrue, Anne Dieux-Coeslier, Tomonobu Hasegawa, Eva E. Holmberg, Rainer Koenig, Gabriele Krueger, Ina Schanze, Eva Seemanova, Adam C. Shaw, Julie Vogt, Marianne Volleth, André Reis, Peter Meinecke, Raoul C.M. Hennekam, Martin Zenker

Research output: Contribution to journal › Article › peer-review

21 Citations (Scopus)

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